XERODERMA PIGMENTOSUM IN A NEGRESS

Xeroderma Pigmentosum M L Kulkarni K saniay Kani Xeroderma pigmehtosum (XP) is a rare autosomal recessive disorder associated with defective DNA repair which causes photosensitivity The photosensitivity leads to pigmentary changes, atrophy and later squamous cell carcinoma of the skin(l) So far

A Case of Xeroderma Pigmentosum - Biomedresus

Xeroderma pigmentosum is a very rare disease, which is said to affect one in a million of the population, scientific studies cannot be carried out on this particular aspect However, it should also be taken into consideration that case reports like this one also present scientific evidence I have so far published several articles on this case

Xeroderma Pigmentosum Cells Contain LowLevels

Xeroderma pigmentosum is a rare disease in which affected individuals develop pigmentation abnormalities and malig-nant growth in regions of skin exposed to sunlight (1) Cells from most xeroderma patients are deficient in the unsched-uled DNA synthesis elicited by ultraviolet light (220-300 nm) in normal cells (2); these cells are thought to

Xeroderma Pigmentosum: A Case Report - AAPD

398 Park, Dock Xeroderma pigmentosum Pediatric Dentistry – 25:4, 2003 eventually leads to malig-nant growths Prevention and early treatment can limit the problems that arise The purpose of this article is to inform the den-tal practitioner of the precautions necessary when treating these patients Case report A 10-year-old boy with a

Xeroderma Pigmentosum: A Retrospective Case Series in Zimbabwe

Xeroderma pigmentosum (XP) is a rare autosomal recessively transmitted genetic disease characterized by clinical and cellular sensitivity to ultraviolet (UV) radiation 1-5 Patients with this disease show hypersen-sitivity to sunlight and extreme susceptibility to sun-light-induced cutaneous cancers 1-5 XP also is associ-